Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed res...
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paper:paper_00404020_v58_n21_p4237_DiSalvo2023-06-08T15:04:15Z Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ Di Salvo, Florencia Crespo, Alejandro Estrin, Dario Ariel Doctorovich, Fabio Ariel 2,2,2-trifluoroethylamine Complex Density functional theory Electron transfer n-butylamine Nitrosyl Ruthenium 2,2,2 trifluoroethylamine butylamine ethylamine ruthenium complex unclassified drug article calculation chemical reaction complex formation electron transport molecular stability priority journal reaction analysis solvation theory The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed results suggest that stabilization of the trifluoroethyldiazonium ion by complexation is much larger than the one corresponding to the butyl ion, in agreement with the fact that no rearrangement products derived from CF3CH2+ were observed. © 2002 Elsevier Science Ltd. All rights reserved. Fil:Di Salvo, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Crespo, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Estrin, D.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Doctorovich, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v58_n21_p4237_DiSalvo http://hdl.handle.net/20.500.12110/paper_00404020_v58_n21_p4237_DiSalvo |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
2,2,2-trifluoroethylamine Complex Density functional theory Electron transfer n-butylamine Nitrosyl Ruthenium 2,2,2 trifluoroethylamine butylamine ethylamine ruthenium complex unclassified drug article calculation chemical reaction complex formation electron transport molecular stability priority journal reaction analysis solvation theory |
spellingShingle |
2,2,2-trifluoroethylamine Complex Density functional theory Electron transfer n-butylamine Nitrosyl Ruthenium 2,2,2 trifluoroethylamine butylamine ethylamine ruthenium complex unclassified drug article calculation chemical reaction complex formation electron transport molecular stability priority journal reaction analysis solvation theory Di Salvo, Florencia Crespo, Alejandro Estrin, Dario Ariel Doctorovich, Fabio Ariel Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
topic_facet |
2,2,2-trifluoroethylamine Complex Density functional theory Electron transfer n-butylamine Nitrosyl Ruthenium 2,2,2 trifluoroethylamine butylamine ethylamine ruthenium complex unclassified drug article calculation chemical reaction complex formation electron transport molecular stability priority journal reaction analysis solvation theory |
description |
The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed results suggest that stabilization of the trifluoroethyldiazonium ion by complexation is much larger than the one corresponding to the butyl ion, in agreement with the fact that no rearrangement products derived from CF3CH2+ were observed. © 2002 Elsevier Science Ltd. All rights reserved. |
author |
Di Salvo, Florencia Crespo, Alejandro Estrin, Dario Ariel Doctorovich, Fabio Ariel |
author_facet |
Di Salvo, Florencia Crespo, Alejandro Estrin, Dario Ariel Doctorovich, Fabio Ariel |
author_sort |
Di Salvo, Florencia |
title |
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
title_short |
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
title_full |
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
title_fullStr |
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
title_full_unstemmed |
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ |
title_sort |
reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [ru(bpy)2(no)cl]2+ |
publishDate |
2002 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v58_n21_p4237_DiSalvo http://hdl.handle.net/20.500.12110/paper_00404020_v58_n21_p4237_DiSalvo |
work_keys_str_mv |
AT disalvoflorencia reactionpathwaysof222trifluoroethylamineandnbutylaminewithrubpy2nocl2 AT crespoalejandro reactionpathwaysof222trifluoroethylamineandnbutylaminewithrubpy2nocl2 AT estrindarioariel reactionpathwaysof222trifluoroethylamineandnbutylaminewithrubpy2nocl2 AT doctorovichfabioariel reactionpathwaysof222trifluoroethylamineandnbutylaminewithrubpy2nocl2 |
_version_ |
1768543362268266496 |